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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298662Generated: October 31, 2026

4-Cyclohexylphenylthiourea → HCID 86583848, compound

https://huagongshe.com/reaction/2298662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyclohexylphenylthioureaHCID 2732180—
ReactantMethyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylateHCID 86583828—
ProductHCID 86583848HCID 8658384842.1%

Reaction Steps

Methyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylate (65 mg, 0.21 mmol) was allowed to react with 4-cyclohexylphenylthiourea (49.2 mg) as described in Example 154, step (a) to give 45 mg (41% yield) of methyl 4-{2-[(4-cyclohexylphenyl)amino](1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxylate hydrobromide. 1H NMR (DMSO-d6, 300 MHz) δ1.23-1.39 (m, 5H), 1.71-1.79 (m, 5H), 2.68 (s, 3H), 3.83 (s, 3H), 7.16 (d, 2H, J=8.6 Hz), 7.26 (s, 1H), 7.65 (d, 2H, J=8.7 Hz), 8.14 (s, 1H), 10.19 (s, 1H); Mass Spectrum (ESI) m/z calcd. for C22H24N2O2S3, 444.64 (M+H), found 445.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-51376fdc168344228f54362868434cf3
Source noteuspto-grants-2002_12